510(k) Report

FDA applicant

Touch Scientific, Inc.

Raleigh, NC3 decisions1993–19990 recalls

FDA records 3 decisions for Touch Scientific, Inc. (Raleigh, NC) from 1993 to 1999: 3 510(k) clearances. Most are in product codes DEG (Lactoferrin, Antigen, Antiserum, Control) and DGC (Ige, Antigen, Antiserum, Control). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, immunology panel, where it files most

How often FDA has decided Touch Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Touch Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Touch Scientific, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DEGLactoferrin, Antigen, Antiserum, Control2decisions
  • DGCIge, Antigen, Antiserum, Control1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K991316Touch Tear Ige Microassay KitTouch Scientific, Inc. · 19991cites it

What has FDA decided for it lately?

  • K991316Touch Tear Ige Microassay KitTouch Scientific, Inc. · 1999
  • K934473Lactoferrin Microassay SystemTouch Scientific, Inc. · 1993
  • K931901LactocardTouch Scientific, Inc. · 1993

All 3 as Touch Scientific, Inc. →

Other applicant names beginning “Touch”

FDA records each applicant name separately; these may or may not be the same firm.

Touch Medical Solutions, Inc. 1Touch Corp. 1